Zhandong Liu

Human-specific regulation of MeCP2 levels in fetal brains by microRNA miR-483-5p.

Digital sorting of complex tissues for cell type-specific gene expression profiles.

Expression and Functional Pathway Analysis of Nuclear Receptor NR2F2 in Ovarian Cancer.

NLRP7 affects trophoblast lineage differentiation, binds to overexpressed YY1 and alters CpG methylation.

Combinatorial therapy discovery using mixed integer linear programming.

On the reproducibility of TCGA ovarian cancer microRNA profiles.

Molecular pathway identification using biological network-regularized logistic models.

Serine catabolism regulates mitochondrial redox control during hypoxia.

A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases.

FOXG1 expression shows correlation with neuronal differentiation in cerebellar development, aggressive phenotype in medulloblastomas, and survival in a xenograft model of medulloblastoma.

TCGA2STAT: simple TCGA data access for integrated statistical analysis in R.

Post-transcriptional regulation of SHANK3 expression by microRNAs related to multiple neuropsychiatric disorders.

Reversal of phenotypes in MECP2 duplication mice using genetic rescue or antisense oligonucleotides.

Crowdsourced estimation of cognitive decline and resilience in Alzheimer's disease.

Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.

Graphical Models via Univariate Exponential Family Distributions.

XMRF: an R package to fit Markov Networks to high-throughput genetics data.

Transcriptomic Analysis of Mouse Cochlear Supporting Cell Maturation Reveals Large-Scale Changes in Notch Responsiveness Prior to the Onset of Hearing.

Extensive cryptic splicing upon loss of RBM17 and TDP43 in neurodegeneration models.

Transcriptional Regulation by ATOH1 and its Target SPDEF in the Intestine.

Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans.

Comprehensive evaluation of RNA-seq quantification methods for linearity.

MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.

CRISPRcloud: a secure cloud-based pipeline for CRISPR pooled screen deconvolution.

Disease-related gene module detection based on a multi-label propagation clustering algorithm.

A Role for Progesterone-Regulated sFRP4 Expression in Uterine Leiomyomas.

Data Analysis Pipeline for RNA-seq Experiments: From Differential Expression to Cryptic Splicing.

The International Conference on Intelligent Biology and Medicine (ICIBM) 2016: from big data to big analytical tools.

The International Conference on Intelligent Biology and Medicine (ICIBM) 2016: summary and innovation in genomics.

An ultra-fast and scalable quantification pipeline for transposable elements from next generation sequencing data.

POU6f1 Mediates Neuropeptide-Dependent Plasticity in the Adult Brain.

Loss of Capicua alters early T cell development and predisposes mice to T cell lymphoblastic leukemia/lymphoma.

Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome.

ATXN1-CIC Complex Is the Primary Driver of Cerebellar Pathology in Spinocerebellar Ataxia Type 1 through a Gain-of-Function Mechanism.

Forniceal deep brain stimulation induces gene expression and splicing changes that promote neurogenesis and plasticity.

Detecting hidden batch factors through data-adaptive adjustment for biological effects.

Genome-wide distribution of linker histone H1.0 is independent of MeCP2.

Epigenetic drift of H3K27me3 in aging links glycolysis to healthy longevity in .

Tau Activates Transposable Elements in Alzheimer's Disease.

High-Throughput Functional Analysis Distinguishes Pathogenic, Nonpathogenic, and Compensatory Transcriptional Changes in Neurodegeneration.

Apparent bias toward long gene misregulation in MeCP2 syndromes disappears after controlling for baseline variations.

TFEB enhances astroglial uptake of extracellular tau species and reduces tau spreading.

A Druggable Genome Screen Identifies Modifiers of α-Synuclein Levels via a Tiered Cross-Species Validation Approach.

RBM17 Interacts with U2SURP and CHERP to Regulate Expression and Splicing of RNA-Processing Proteins.

Complement C3aR Inactivation Attenuates Tau Pathology and Reverses an Immune Network Deregulated in Tauopathy Models and Alzheimer's Disease.

Metabolomics of mammalian brain reveals regional differences.

An autism-linked missense mutation in SHANK3 reveals the modularity of Shank3 function.

Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus-CA3 projection.

A kinome-wide RNAi screen identifies ERK2 as a druggable regulator of Shank3 stability.

Beta-binomial modeling of CRISPR pooled screen data identifies target genes with greater sensitivity and fewer false negatives.

Author Correction: Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus-CA3 projection.